FDA inspection
Aktina Medical Corp: FDA inspection ending Jul 24, 2017
FDA inspection 1018921 · Voluntary Action Indicated (VAI) · Congers, NY
Key facts
| Inspection ID | 1018921 |
|---|---|
| Firm | Aktina Medical Corp |
| FEI number | 1000521490 |
| Address | 360 N Route 9W |
| City | Congers |
| State | NY |
| ZIP | 10920 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jul 24, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data